This lesson describes the uses and implications of pre-implantation genetic diagnosis, amniocentesis and chorionic villus sampling. The lesson PowerPoint and accompanying worksheets have been primarily designed to cover point 2.15 of the Pearson Edexcel A-level Biology A (Salters Nuffield) specification but regular links are made to the earlier content of topics 1 & 2, and their knowledge of topics including the heart and circulation, monohybrid inheritance and cystic fibrosis are tested.
The lesson begins by challenging them to use this prior knowledge of topic 2 to identify the letters in the abbreviations PGD and CVS. The involvement of IVF to obtain the embryos (or oocytes) is then discussed and a series of exam-style questions are used to get them to understand how this method screens embryos prior to implantation, so that those identified as having genetic diseases or being carriers are not inserted into the female’s uterus. Mark schemes for all of the questions included in this lesson are embedded into the PowerPoint so students can constantly assess their progress.
Moving forwards, Down syndrome (trisomy 21) is used as an example of a chromosomal abnormality that can be tested for using CVS or amniocentesis. Time is taken to describe the key details of both of these procedures so students have a clear understanding of the implications and the invasiveness to the female being tested. The link between amniocentesis and an increased risk of miscarriage is considered and the results of a 2006 study are used to challenge them on their data skills.
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Nucleic acids, Genetics and Inheritance (Edexcel SNAB)
This lesson bundle contains 16 lessons which have been designed to cover the Pearson Edexcel A-level Biology A (Salters Nuffield) specification points which focus on the structure of DNA and RNA, their roles in replication and protein synthesis, and genetics and inheritance. The lesson PowerPoints are highly detailed, and along with their accompanying worksheets, they have been planned at length to contain a wide range of engaging tasks which cover the following A-level Biology content found in topics 2, 3 and 6 of the course: 2.5 (i): Know the basic structure of mononucleotides (deoxyribose or ribose linked to a phosphate and a base, including thymine, uracil, cytosine, adenine or guanine) and the structures of DNA and RNA (polynucleotides composed of mononucleotides linked through condensation reactions) 2.5 (ii): Know how complementary base pairing and the hydrogen bonding between two complementary strands are involved in the formation of the DNA double helix 2.6 (i): Understand the process of protein synthesis (transcription) including the role of RNA polymerase, translation, messenger RNA, transfer RNA, ribosomes and the role of start and stop codons 2.6 (ii): Understand the roles of the DNA template (antisense) strand in transcription, codons on messenger RNA and anticodons on transfer RNA 2.7: Understand the nature of the genetic code 2.8: Know that a gene is a sequence of bases on a DNA molecule that codes for a sequence of amino acids in a polypeptide chain 2.11 (i): Understand the process of DNA replication, including the role of DNA polymerase 2.12 (i): Understand how errors in DNA replication can give rise to mutations 2.12 (ii): Understand how cystic fibrosis results from one of a number of possible gene mutations 2.13 (i): Know the meaning of the terms: gene, allele, genotype, phenotype, recessive, dominant, incomplete dominance, homozygote and heterozygote 2.13 (ii): Understand patterns of inheritance, including the interpretation of genetic pedigree diagrams, in the context of monohybrid inheritance 2.14: Understand how the expression of a gene mutation in people with cystic fibrosis impairs the functioning of the gaseous exchange, digestive and reproductive systems 2.15 (i): Understand the uses of genetic screening, including the identification of carriers, pre-implantation genetic diagnosis (PGD) and prenatal testing, including amniocentesis and chorionic villus sampling 2.15 (ii): Understand the implications of prenatal genetic screening 3.8 (i): The loci is a location of genes on a chromosome 3.8 (ii): The linkage of genes on a chromosome and sex linkage 3.12: Understand how cells become specialised through differential gene expression, producing active mRNA leading to synthesis of proteins, which in turn control cell processes or determine cell structure in animals and plants, including the lac operon 3.14 (i): Phenotype is an interaction between genotype and the environment 3.15: Understand how some phenotypes are affected by multiple alleles for the same gene at many loci (polygenic inheritance) as well as the environment and how this can give rise to phenotypes that show continuous variation 6.4: Know how DNA can be amplified using the polymerase chain reaction (PCR) 6.10: Understand how one gene can give rise to more than one protein through posttranscriptional changes to messenger RNA (mRNA).
£18.00
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Topic 2: Genes and Health (Pearson Edexcel SNAB)
Some of the key biological topics are covered in topic 2 of the Pearson Edexcel A-level Biology A (Salters Nuffield) course and include the transport of materials across cell membranes, DNA structure and replication, protein synthesis and monohybrid inheritance. In line with this, many hours of intricate planning have gone into the design of all of the 19 lessons that are included in this bundle to ensure that the content is covered in detail, understanding is constantly checked to immediately address misconceptions and that engagement is high. This is achieved through the wide variety of tasks in the PowerPoints and accompanying worksheets which include exam-style questions with clear answers, discussion points, differentiated tasks and quick quiz competitions. The following specification points are covered by the lessons within this bundle: * The properties of gas exchange surfaces in living organisms * Understand how the rate of diffusion is dependent on these properties and can be used in the calculation of the rate of diffusion by Fick's law * Adaptations of the mammalian lung for rapid gaseous exchange * Structure and properties of cell membranes * Simple and facilitated diffusion as methods of passive transport * The involvement of ATP and carrier proteins in active transport, endocytosis and exocytosis * The basic structure of mononucleotides * The structures of DNA and RNA * The process of protein synthesis * The roles of the template strand, mRNA and tRNA * The nature of the genetic code * A gene is a sequence of bases on DNA that codes for the amino acid sequence of a polypeptide * The basic structure of an amino acid * The formation of polypeptides and proteins * The primary, secondary, tertiary and quaternary structure of proteins * Globular and fibrous proteins using haemoglobin and collagen as examples * The mechanism of action and the specificity of enzymes * Enzymes are biological catalysts that reduce activation energy * The process of DNA replication * Errors in DNA replication can give rise to mutations * The meaning of key genetic terms * Patterns of inheritance, in the context of monohybrid inheritance * Understand how the expression of a gene mutation in people with cystic fibrosis impairs the functioning of the gaseous exchange, digestive and reproductive systems * Understand the uses and implications of genetic screening and prenatal testing Due to the detail included in each of these lessons, it is estimated that it will take in excess of 2 months of allocated teaching time to cover the content. If you would like to see the quality of the lessons, download the gas exchange surfaces, cell membranes, transcription, globular and fibrous proteins, monohybrid inheritance and cystic fibrosis lessons as these have been shared for free
£23.00
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